ANVISA registration 10230730215Valid until Jun 08, 2036

YELLOW FEVER

Name: YELLOW FEVER — ANVISA registration 10230730215
Creator: NL COMÉRCIO EXTERIOR LTDA
Keywords: YELLOW FEVER, FEBRE AMARELA, Teste Rápido Febre Amarela IgG/IgM, 10230730215, Risk Class III, ANVISA registration

ANVISA Registration Number: 10230730215NL COMÉRCIO EXTERIOR LTDANL COMÉRCIO EXTERIOR LTDARisk Class III

Verified

Device names

Technical name: YELLOW FEVER
Commercial name: Teste Rápido Febre Amarela IgG/IgM
Risk class: Class III

Registration details

Registration Number: 10230730215
Process Number: 25351001688202633
CNPJ: 52541273000147

Company information

Registration Holder: NL COMÉRCIO EXTERIOR LTDA
Manufacturer: NL COMÉRCIO EXTERIOR LTDA
Manufacturing Country: Brazil

Dates and status

Publication Date: Jun 08, 2026
Validity: 08/06/2036
Last Updated: 08/18/2026 19:00:00

About this record

Access comprehensive regulatory information for YELLOW FEVER in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10230730215 and manufactured by NL COMÉRCIO EXTERIOR LTDA. The registration is held by NL COMÉRCIO EXTERIOR LTDA with validity until Jun 08, 2036.

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